Other names |
BHV-3000, BMS-927711 |
MK-1602 |
AGN-241689, MK-8031 |
Trade name |
Nurtec®, Nurtec ODT®, Vydura® |
Ubrelvy®
|
Qulipta®
|
Marketed |
Biohaven Pharmaceuticals, Pfizer |
Allergan Pharmaceuticals |
Allergan Pharmaceuticals |
FDA approval |
February 2020 (acute); May 2021 (prevention) |
December 2019 |
September 2021 |
Molecule |
|
|
|
Indication |
Acute treatment of migraine with or without aura in adults. Preventive treatment of episodic migraine in adults |
Acute treatment of migraine with or without aura in adults |
Preventive treatment of episodic migraine in adults |
Dose |
75 mg PO as needed. Not to exceed 75 mg/ 24 h. Safety of >18 doses/30 days has not been established |
50 or 100 mg PO as needed. If needed, may take second dose at least 2 hrs after initial dose. Not to exceed 200 mg/24 h. Safety of treating >8 migraines/30 days has not been established |
10, 30, or 60 mg PO |
Dose adjustments |
Renal impairment (CrCl < 15 mL/min); hepatic impairment (Child–Pugh > C); drug interactions |
Renal impairment (CrCl < 30 mL/min); hepatic impairment (Child–Pugh ≥ C); drug interactions |
Renal impairment (CrCl < 30 mL/min); hepatic impairment (Child–Pugh ≥ C); drug interactions |
Route of administration |
Oral |
Oral |
Oral |
Contraindications |
History of hypersensitivity |
Concomitant use with strong CYP3A4 inhibitors |
None |
Adverse effects |
Nausea (2%), hypersensitivity (including delayed) |
Nausea (2–4%), somnolence (2–3%), dry mouth (2%) |
Nausea (5–9%), constipation (6%), somnolence (4–6%), elevated AST/ALT (1%) |
Pregnancy and lactation |
Data not available |
Data not available |
Data not available |
Pediatric |
Data not available |
Data not available |
Data not available |
Considerations |
Orally disintegrating tablet. It can be swallowed without additional liquid |
High-fat meal delayed plasma concentration |
High-fat meal effect was not significant. |